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[托西拉酯(IPD-1151T)对I-IV型过敏反应的影响]

[Effect of suplatast tosilate (IPD-1151T) on types I-IV allergic reactions].

作者信息

Matsuura N, Mori H, Nagai H, Koda A

机构信息

Department of Pharmacology, Gifu Pharmaceutical University, Japan.

出版信息

Nihon Yakurigaku Zasshi. 1992 Dec;100(6):495-501. doi: 10.1254/fpj.100.495.

Abstract

We examined the effect of suplatast tosilate (IPD-1151T), which exhibits a class-specific suppression of IgE antibody production, on types I-IV allergic reactions. 1) Type I reaction: IPD-1151T dose-dependently inhibited 48-hr homologous passive cutaneous anaphylaxis (PCA) when the agent was given p.o. 30 min prior to the antigen challenge. To observe the time course of the inhibitory activity, IPD-1151T in a dose of 50 mg/kg was given orally at various times prior to the antigen challenge. IPD-1151T showed inhibitory activity when it was given at 0.5 to 2 hr prior to the antigen challenge, and the maximum inhibition was found when the IPD-1151T pretreatment was 2-hr before the challenge. IPD-1151T also suppressed the antigen-induced degranulation of mesenteric mast cells and histamine release from peritoneal exudate cells of rats. 2) Type II reaction: Only a high dose of IPD-1151T given orally inhibited reversed cutaneous anaphylaxis in rats, whereas the agent did not affect Forssman shock in guinea pigs. 3) Types III and IV reactions: IPD-1151T neither affected the Arthus reaction in rabbits nor the picryl chloride-induced contact dermatitis and sheep erythrocytes-induced footpad reaction in mice. The results obtained here indicate that IPD-1151T shows a relatively specific suppression of the type I allergic reaction with the inhibition of degranulation and histamine release from mast cells.

摘要

我们研究了对甲苯磺酸盐舒普拉泰(IPD - 1151T)对I - IV型过敏反应的影响,该药物对IgE抗体产生具有类别特异性抑制作用。1)I型反应:当在抗原攻击前30分钟口服给予IPD - 1151T时,其剂量依赖性地抑制了48小时同源被动皮肤过敏反应(PCA)。为了观察抑制活性的时间进程,在抗原攻击前的不同时间口服给予50mg/kg剂量的IPD - 1151T。当在抗原攻击前0.5至2小时给予IPD - 1151T时显示出抑制活性,当IPD - 1151T预处理在攻击前2小时时发现最大抑制作用。IPD - 1151T还抑制了抗原诱导的大鼠肠系膜肥大细胞脱颗粒和腹膜渗出细胞组胺释放。2)II型反应:仅口服给予高剂量的IPD - 1151T可抑制大鼠的反向皮肤过敏反应,而该药物对豚鼠的福斯曼休克无影响。3)III型和IV型反应:IPD - 1151T既不影响兔的阿瑟斯反应,也不影响小鼠的苦味酸诱导的接触性皮炎和绵羊红细胞诱导的足垫反应。此处获得的结果表明,IPD - 1151T对I型过敏反应表现出相对特异性的抑制作用,同时抑制肥大细胞脱颗粒和组胺释放。

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